4.6 Article

About the selectivity and reactivity of active nickel electrodes in C-C coupling reactions

Journal

RSC ADVANCES
Volume 10, Issue 24, Pages 14249-14253

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ra02673e

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Funding

  1. Advanced Lab of Electrochemistry and Electrosynthesis ELYSION (Carl-Zeiss-Stiftung)
  2. DFG fellowship through the Excellence Initiative, Graduate School Materials Science in Mainz [GSC 266]

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Active anodes which are operating in highly stable protic media such as 1,1,1,3,3,3-hexafluoroisopropanol are rare. Nickel forms, within this unique solvent, a non-sacrificial active anode at constant current conditions, which is superior to the reported powerful molybdenum system. The reactivity for dehydrogenative coupling reactions of this novel active anode increases when the electrolyte is not stirred during electrolysis. Besides the aryl-aryl coupling, a dehydrogenative arylation reaction of benzylic nitriles was found while stirring the mixture providing quick access to synthetically useful building blocks.

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